Colon Cancer: Gene >> ERRFI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8013372:8013372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779337445
CDS Mutation	c.1227A>T
AA Mutation	p.Lys409Asn(p.K409N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8013822:8013822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777G>T
AA Mutation	p.Lys259Asn(p.K259N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8014298:8014298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301G>A
AA Mutation	p.Glu101Lys(p.E101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8014193:8014193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406T>C
AA Mutation	p.Ser136Pro(p.S136P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8013836:8013836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763G>C
AA Mutation	p.Gly255Arg(p.G255R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8013868:8013868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746056102
CDS Mutation	c.731G>A
AA Mutation	p.Arg244Gln(p.R244Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8015344:8015344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166C>A
AA Mutation	p.Leu56Met(p.L56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8013338:8013338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201286989
CDS Mutation	c.1261G>A
AA Mutation	p.Ala421Thr(p.A421T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377482
Start	8014011:8014011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ERRFI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377482
Start	8013374:8013374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225A>C
AA Mutation	p.Lys409Gln(p.K409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript